24 results · 25ms · Sources: EU EUDAMED, US FDA

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IMMAGE SYSTEMS TOTAL IMMUNOGLOBULIN E (IGE) REAGENT IMMAGE IGE CALIBRATOR

FDA 510(k)
FDA Class 2 ·Immunology

Safco Flexible Files

FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310242103·Safco flexible files #20 21mm 6/box

APEX Revision Knee

FDA UDI
Omni Life Science, Inc.·00841690113942·PS-R Insert, Size 2 x 10mm

Max-Vac Evacuator Tips Unscented

FDA UDI
PRACTICON, INC.·00723896009819·offer two unique ends for a super low price - u...

Navagio

FDA UDI
Kalitec Direct LLC·B07330K0142100·Trial, TLIF, 32L OB CRV 7Deg, 10mm

GLUCOMETER DEX BLOOD GLUCOSE SYSTEM (MODIFIED)

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

PALMO THERMOREGULATION INTERFACE ACCESSORY

FDA 510(k)
FDA Class 2 ·Cardiovascular

BD VACUTAINER® BORIC ACID SODIUM BORATE/FORMATE C&S URINE TUBE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code JSM·April 25, 2018

MECHANICAL CHAIR/TRANSPORT CHAIR

FDA Adverse Event
Malfunction ·UNKNOWN·Product code INM·March 27, 2013

COUGAR XT STEERABLE GUIDEWIRE

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code DQX·March 3, 2011

LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 LARGE TITANIUM LAGATING

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code FZP·March 27, 2008

FOLYSIL SILICONE CATHETER

FDA Adverse Event
Malfunction ·COLOPLAST A/S·Product code EZL·October 30, 2024

FOLYSIL SILICONE CATHETER

FDA Adverse Event
Malfunction ·COLOPLAST A/S·Product code EZL·November 19, 2024

MICRA

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code DYB·January 24, 2024

MICRA AV

FDA Adverse Event
Death ·MEDTRONIC IRELAND·Product code PNJ·January 24, 2024

MICRA

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code PNJ·January 24, 2024

MICRA

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code PNJ·January 24, 2024

MICRA

FDA Adverse Event
Death ·MEDTRONIC IRELAND·Product code PNJ·January 24, 2024

FOLYSIL SILICONE CATHETER

FDA Adverse Event
Malfunction ·COLOPLAST A/S·Product code EZL·November 26, 2024

ARROW CVC SET: 2-LUMEN 4 FR X 5 CM

FDA Adverse Event
Malfunction ·ARROW INTERNATIONAL LLC·Product code DQY·September 10, 2024